| 1 | [SID26730032] | Active | | | Aqueous Solubility from MLSMR Stock Solutions [AID1996, Type: other] | |  View X | Row No. | 1 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Active | | BioAssay | Aqueous Solubility from MLSMR Stock Solutions | | AID | 1996 | | BioAssay type | other | | Target | | | PubMed | | | Data Table |  |
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| 2 | [SID26730032] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 2 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
|
| 3 | [SID26730032] | Unspecified | Potency | | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate [AID624178, Type: confirmatory] | acid sphingomyelinase [Homo sapiens] [gi:179095] |  View X | Row No. | 3 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Unspecified | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Human Acid Sphingomyelinase Assay: Native Substrate | | AID | 624178 | | BioAssay type | confirmatory | | Target | acid sphingomyelinase [Homo sapiens] [gi:179095] | | PubMed | | | Data Table |  |
|
| 4 | [SID26730032] | Inactive | Potency | 31.6228 | qHTS for Inhibitors of ATXN expression [AID651635, Type: confirmatory] | ATXN2 gene product [Homo sapiens] [gi:171543895] |  View X | Row No. | 4 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | Potency | 31.6228 [uM] | | BioAssay | qHTS for Inhibitors of ATXN expression | | AID | 651635 | | BioAssay type | confirmatory | | Target | ATXN2 gene product [Homo sapiens] [gi:171543895] | | PubMed | | | Data Table |  |
|
| 5 | [SID26730032] | Inactive | EC50 | 110 | Luminescence-based Microorganism Dose Response HTS to Identify Inhibitors of E. Coli Growth [AID1959, Type: confirmatory] | |  View X | Row No. | 5 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | EC50 | 110 [uM] | | BioAssay | Luminescence-based Microorganism Dose Response HTS to Identify Inhibitors of E. Coli Growth | | AID | 1959 | | BioAssay type | confirmatory | | Target | | | PubMed | | | Data Table |  |
|
| 6 | [SID26730032] | Inactive | EC50 | 300 | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 [AID1960, Type: confirmatory] | Zinc finger protein mex- [gi:55976631] |  View X | Row No. | 6 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | EC50 | 300 [uM] | | BioAssay | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 | | AID | 1960 | | BioAssay type | confirmatory | | Target | Zinc finger protein mex- [gi:55976631] | | PubMed | | | Data Table |  |
|
| 7 | [SID26730032] | Inactive | EC50 | 300 | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 [AID1960, Type: confirmatory] | Zinc finger protein mex- [gi:55976631] |  View X | Row No. | 7 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | EC50 | 300 [uM] | | BioAssay | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of Mex-5 Binding to TCR-2 | | AID | 1960 | | BioAssay type | confirmatory | | Target | Zinc finger protein mex- [gi:55976631] | | PubMed | | | Data Table |  |
|
| 8 | [SID26730032] | Inactive | EC50 | 300 | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of POS-1 Binding to mex-3-RNA [AID1964, Type: confirmatory] | POsterior Segregation family member (pos-1) [Caenorhabditis elegans] [gi:17562800] |  View X | Row No. | 8 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | EC50 | 300 [uM] | | BioAssay | Fluorescent Polarization Homogeneous Dose Response HTS to Indentify Inhibitors of POS-1 Binding to mex-3-RNA | | AID | 1964 | | BioAssay type | confirmatory | | Target | POsterior Segregation family member (pos-1) [Caenorhabditis elegans] [gi:17562800] | | PubMed | | | Data Table |  |
|
| 9 | [SID26730032] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify activators of the DAF-12 from the parasite S. stercoralis (ssDAF-12) [AID652126, Type: screening] | Protein DAF-12, isoform a [Caenorhabditis elegans] [gi:71987181] |  View X | Row No. | 9 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify activators of the DAF-12 from the parasite S. stercoralis (ssDAF-12) | | AID | 652126 | | BioAssay type | screening | | Target | Protein DAF-12, isoform a [Caenorhabditis elegans] [gi:71987181] | | PubMed | | | Data Table |  |
|
| 10 | [SID26730032] | Inactive | | | Luminescence-based cell-based primary high throughput screening assay to identify activators of the DAF-12 from the parasite H. contortus (hcDAF-12) [AID652067, Type: screening] | Protein DAF-12, isoform a [Caenorhabditis elegans] [gi:71987181] |  View X | Row No. | 10 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Luminescence-based cell-based primary high throughput screening assay to identify activators of the DAF-12 from the parasite H. contortus (hcDAF-12) | | AID | 652067 | | BioAssay type | screening | | Target | Protein DAF-12, isoform a [Caenorhabditis elegans] [gi:71987181] | | PubMed | | | Data Table |  |
|
| 11 | [SID26730032] | Inactive | | | uHTS identification of APOBEC3A DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay [AID493011, Type: screening] | APOBEC3A gene product [Homo sapiens] [gi:21955158] |  View X | Row No. | 11 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | uHTS identification of APOBEC3A DNA Deaminase Inhibitors via a fluorescence-based single-stranded DNA deaminase assay | | AID | 493011 | | BioAssay type | screening | | Target | APOBEC3A gene product [Homo sapiens] [gi:21955158] | | PubMed | | | Data Table |  |
|
| 12 | [SID26730032] | Inactive | Potency | | qHTS for Inhibitors of Vif-A3F Interactions: qHTS [AID602313, Type: confirmatory] | APOBEC3F gene product [Homo sapiens] [gi:22907044] |  View X | Row No. | 12 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS for Inhibitors of Vif-A3F Interactions: qHTS | | AID | 602313 | | BioAssay type | confirmatory | | Target | APOBEC3F gene product [Homo sapiens] [gi:22907044] | | PubMed | | | Data Table |  |
|
| 13 | [SID26730032] | Inactive | | | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of human diacylglycerol lipase, beta (DAGLB) [AID504411, Type: screening] | sn1-specific diacylglycerol lipase beta isoform 1 [Homo sapiens] [gi:218931251] |  View X | Row No. | 13 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of human diacylglycerol lipase, beta (DAGLB) | | AID | 504411 | | BioAssay type | screening | | Target | sn1-specific diacylglycerol lipase beta isoform 1 [Homo sapiens] [gi:218931251] | | PubMed | | | Data Table |  |
|
| 14 | [SID26730032] | Inactive | | | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of human diacylglycerol lipase, beta (DAGLB) [AID504411, Type: screening] | sn1-specific diacylglycerol lipase beta isoform 1 [Homo sapiens] [gi:218931251] |  View X | Row No. | 14 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Fluorescence-based primary biochemical high throughput screening assay to identify inhibitors of human diacylglycerol lipase, beta (DAGLB) | | AID | 504411 | | BioAssay type | screening | | Target | sn1-specific diacylglycerol lipase beta isoform 1 [Homo sapiens] [gi:218931251] | | PubMed | | | Data Table |  |
|
| 15 | [SID26730032] | Inactive | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. [AID1947, Type: screening] | Fam108b protein [Mus musculus] [gi:21595511] |  View X | Row No. | 15 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. | | AID | 1947 | | BioAssay type | screening | | Target | Fam108b protein [Mus musculus] [gi:21595511] | | PubMed | | | Data Table |  |
|
| 16 | [SID26730032] | Inactive | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. [AID1947, Type: screening] | Fam108b protein [Mus musculus] [gi:21595511] |  View X | Row No. | 16 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. | | AID | 1947 | | BioAssay type | screening | | Target | Fam108b protein [Mus musculus] [gi:21595511] | | PubMed | | | Data Table |  |
|
| 17 | [SID26730032] | Inactive | | | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. [AID1947, Type: screening] | Fam108b protein [Mus musculus] [gi:21595511] |  View X | Row No. | 17 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based counterscreen for RBBP9 inhibitors: primary biochemical high throughput screening assay to identify inhibitors of the serine hydrolase family member Fam108B. | | AID | 1947 | | BioAssay type | screening | | Target | Fam108b protein [Mus musculus] [gi:21595511] | | PubMed | | | Data Table |  |
|
| 18 | [SID26730032] | Inactive | | | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors of ADP-ribosylation factor GTPase activating protein 1 (ARFGAP1) [AID651572, Type: screening] | Arfgap1 gene product [Rattus norvegicus] [gi:21489979] |  View X | Row No. | 18 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based biochemical primary high throughput screening assay to identify inhibitors of ADP-ribosylation factor GTPase activating protein 1 (ARFGAP1) | | AID | 651572 | | BioAssay type | screening | | Target | Arfgap1 gene product [Rattus norvegicus] [gi:21489979] | | PubMed | | | Data Table |  |
|
| 19 | [SID26730032] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that activate MrgX1 receptor signaling [AID588627, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 19 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that activate MrgX1 receptor signaling | | AID | 588627 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
|
| 20 | [SID26730032] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that activate MrgX1 receptor signaling [AID588627, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 20 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that activate MrgX1 receptor signaling | | AID | 588627 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
|
| 21 | [SID26730032] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that allosterically activate MrgX1 receptor signaling [AID588675, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 21 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that allosterically activate MrgX1 receptor signaling | | AID | 588675 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
|
| 22 | [SID26730032] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that allosterically activate MrgX1 receptor signaling [AID588675, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 22 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that allosterically activate MrgX1 receptor signaling | | AID | 588675 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
|
| 23 | [SID26730032] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling [AID588676, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 23 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | | AID | 588676 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
|
| 24 | [SID26730032] | Inactive | | | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling [AID588676, Type: screening] | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] |  View X | Row No. | 24 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening for identification of compounds that antagonize MrgX1 receptor signaling | | AID | 588676 | | BioAssay type | screening | | Target | MAS-related GPR member X1 [Homo sapiens] [gi:195969650] | | PubMed | | | Data Table |  |
|
| 25 | [SID26730032] | Inactive | | | Absorbance-based biochemical primary high throughput screening assay to identify inhibitors of Methionine sulfoxide reductase A (MsrA) [AID651718, Type: screening] | MSRA protein [Bos taurus] [gi:73586699] |  View X | Row No. | 25 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Absorbance-based biochemical primary high throughput screening assay to identify inhibitors of Methionine sulfoxide reductase A (MsrA) | | AID | 651718 | | BioAssay type | screening | | Target | MSRA protein [Bos taurus] [gi:73586699] | | PubMed | | | Data Table |  |
|
| 26 | [SID26730032] | Inactive | | | Absorbance-based biochemical primary high throughput screening assay to identify activators of Methionine sulfoxide reductase A (MsrA) [AID602163, Type: screening] | MSRA protein [Bos taurus] [gi:73586699] |  View X | Row No. | 26 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Absorbance-based biochemical primary high throughput screening assay to identify activators of Methionine sulfoxide reductase A (MsrA) | | AID | 602163 | | BioAssay type | screening | | Target | MSRA protein [Bos taurus] [gi:73586699] | | PubMed | | | Data Table |  |
|
| 27 | [SID26730032] | Inactive | | | uHTS for 14-3-3/Bad interaction inhibitors [AID781, Type: screening] | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide [Bos taurus [gi:27807367] |  View X | Row No. | 27 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | uHTS for 14-3-3/Bad interaction inhibitors | | AID | 781 | | BioAssay type | screening | | Target | tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, zeta polypeptide [Bos taurus [gi:27807367] | | PubMed | | | Data Table |  |
|
| 28 | [SID26730032] | Inactive | | | Primary cell-based high-throughput screening assay to identify agonists of the transient receptor potential channel N1 (TRPN1) [AID1424, Type: screening] | transient receptor potential cation channel, subfamily N, member 1 [Danio rerio] [gi:34330186] |  View X | Row No. | 28 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Primary cell-based high-throughput screening assay to identify agonists of the transient receptor potential channel N1 (TRPN1) | | AID | 1424 | | BioAssay type | screening | | Target | transient receptor potential cation channel, subfamily N, member 1 [Danio rerio] [gi:34330186] | | PubMed | | | Data Table |  |
|
| 29 | [SID26730032] | Inactive | Potency | | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction [AID1461, Type: confirmatory] | NPSR1 gene product [Homo sapiens] [gi:46395496] |  View X | Row No. | 29 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction | | AID | 1461 | | BioAssay type | confirmatory | | Target | NPSR1 gene product [Homo sapiens] [gi:46395496] | | PubMed | | | Data Table |  |
|
| 30 | [SID26730032] | Inactive | Potency | | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction [AID1461, Type: confirmatory] | NPSR1 gene product [Homo sapiens] [gi:46395496] |  View X | Row No. | 30 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | Potency | [uM] | | BioAssay | qHTS Assay for Antagonists of the Neuropeptide S Receptor: cAMP Signal Transduction | | AID | 1461 | | BioAssay type | confirmatory | | Target | NPSR1 gene product [Homo sapiens] [gi:46395496] | | PubMed | | | Data Table |  |
|
| 31 | [SID26730032] | Inactive | | | uHTS for Calpain Inhibitors [AID1236, Type: screening] | calpain II [Sus scrofa] [gi:1628587] |  View X | Row No. | 31 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | uHTS for Calpain Inhibitors | | AID | 1236 | | BioAssay type | screening | | Target | calpain II [Sus scrofa] [gi:1628587] | | PubMed | | | Data Table |  |
|
| 32 | [SID26730032] | Inactive | | | uHTS for Calpain Inhibitors [AID1236, Type: screening] | calpain II [Sus scrofa] [gi:1628587] |  View X | Row No. | 32 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | uHTS for Calpain Inhibitors | | AID | 1236 | | BioAssay type | screening | | Target | calpain II [Sus scrofa] [gi:1628587] | | PubMed | | | Data Table |  |
|
| 33 | [SID26730032] | Inactive | | | uHTS of small molecular inhibitors for p47phox, a regulatory protein of NADPH oxidases (Noxs) [AID1274, Type: screening] | neutrophil cytosolic factor 1 [Homo sapiens] [gi:115298672] |  View X | Row No. | 33 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | uHTS of small molecular inhibitors for p47phox, a regulatory protein of NADPH oxidases (Noxs) | | AID | 1274 | | BioAssay type | screening | | Target | neutrophil cytosolic factor 1 [Homo sapiens] [gi:115298672] | | PubMed | | | Data Table |  |
|
| 34 | [SID26730032] | Inactive | | | In vivo-based yeast HTS to detect compounds rescuing yeast growth/survival of Plasmodium Falciparum HSP40-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-01_Inhibitor_SinglePoint_HTS_Activity [AID504582, Type: screening] | HSP40, subfamily A, putative [Plasmodium falciparum 3D7] [gi:124809271] |  View X | Row No. | 34 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | In vivo-based yeast HTS to detect compounds rescuing yeast growth/survival of Plasmodium Falciparum HSP40-mediated toxicity Measured in Whole Organism System Using Plate Reader - 2120-01_Inhibitor_SinglePoint_HTS_Activity | | AID | 504582 | | BioAssay type | screening | | Target | HSP40, subfamily A, putative [Plasmodium falciparum 3D7] [gi:124809271] | | PubMed | | | Data Table |  |
|
| 35 | [SID26730032] | Inactive | | | Anti-Malarial Hsp90 Inhibitors Measured in Microorganism System Using Plate Reader - 2121-01_Inhibitor_SinglePoint_HTS_Activity_Set2 [AID504621, Type: screening] | HSP90 [Plasmodium falciparum 3D7] [gi:124809506] |  View X | Row No. | 35 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Anti-Malarial Hsp90 Inhibitors Measured in Microorganism System Using Plate Reader - 2121-01_Inhibitor_SinglePoint_HTS_Activity_Set2 | | AID | 504621 | | BioAssay type | screening | | Target | HSP90 [Plasmodium falciparum 3D7] [gi:124809506] | | PubMed | | | Data Table |  |
|
| 36 | [SID26730032] | Inactive | IC50 | | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 36 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) | | AID | 1619 | | BioAssay type | confirmatory | | Target | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] | | PubMed | | | Data Table |  |
|
| 37 | [SID26730032] | Inactive | IC50 | | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 37 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) | | AID | 1619 | | BioAssay type | confirmatory | | Target | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] | | PubMed | | | Data Table |  |
|
| 38 | [SID26730032] | Inactive | IC50 | | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) [AID1619, Type: confirmatory] | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] |  View X | Row No. | 38 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Inhibitors of Plasmodium falciparum M17- Family Leucine Aminopeptidase (M17LAP) | | AID | 1619 | | BioAssay type | confirmatory | | Target | M17 leucyl aminopeptidase [Plasmodium falciparum 3D7] [gi:124809582] | | PubMed | | | Data Table |  |
|
| 39 | [SID26730032] | Inactive | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID1822, Type: screening] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 39 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 1822 | | BioAssay type | screening | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
|
| 40 | [SID26730032] | Inactive | | | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). [AID1822, Type: screening] | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] |  View X | Row No. | 40 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | QFRET-based primary biochemical high throughput screening assay to identify inhibitors of the Plasmodium falciparum M18 Aspartyl Aminopeptidase (PFM18AAP). | | AID | 1822 | | BioAssay type | screening | | Target | M18 aspartyl aminopeptidase [Plasmodium falciparum 3D7] [gi:23505220] | | PubMed | | | Data Table |  |
|
| 41 | [SID26730032] | Inactive | IC50 | | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) [AID1445, Type: confirmatory] | m1-family aminopeptidase [Plasmodium falciparum 3D7] [gi:124512980] |  View X | Row No. | 41 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) | | AID | 1445 | | BioAssay type | confirmatory | | Target | m1-family aminopeptidase [Plasmodium falciparum 3D7] [gi:124512980] | | PubMed | | | Data Table |  |
|
| 42 | [SID26730032] | Inactive | IC50 | | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) [AID1445, Type: confirmatory] | m1-family aminopeptidase [Plasmodium falciparum 3D7] [gi:124512980] |  View X | Row No. | 42 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | IC50 | [uM] | | BioAssay | Inhibitors of Plasmodium falciparum M1- Family Alanyl Aminopeptidase (M1AAP) | | AID | 1445 | | BioAssay type | confirmatory | | Target | m1-family aminopeptidase [Plasmodium falciparum 3D7] [gi:124512980] | | PubMed | | | Data Table |  |
|
| 43 | [SID26730032] | Inactive | | | Multiplex HTS Screen of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae_specifically_ AGP1_MLPCN. [AID2066, Type: screening] | Agp1p [Saccharomyces cerevisiae S288c] [gi:85666113] |  View X | Row No. | 43 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Multiplex HTS Screen of TOR pathway GFP-fusion proteins in Saccharomyes cerevisiae_specifically_ AGP1_MLPCN. | | AID | 2066 | | BioAssay type | screening | | Target | Agp1p [Saccharomyces cerevisiae S288c] [gi:85666113] | | PubMed | | | Data Table |  |
|
| 44 | [SID26730032] | Inactive | | | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of the Ras-converting Enzyme [AID2563, Type: screening] | Rce1p [Saccharomyces cerevisiae S288c] [gi:6323930] |  View X | Row No. | 44 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of the Ras-converting Enzyme | | AID | 2563 | | BioAssay type | screening | | Target | Rce1p [Saccharomyces cerevisiae S288c] [gi:6323930] | | PubMed | | | Data Table |  |
|
| 45 | [SID26730032] | Inactive | | | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of the Ras-converting Enzyme [AID2563, Type: screening] | Rce1p [Saccharomyces cerevisiae S288c] [gi:6323930] |  View X | Row No. | 45 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Fluorescence Cell-Free Homogenous Primary HTS to Identify Inhibitors of the Ras-converting Enzyme | | AID | 2563 | | BioAssay type | screening | | Target | Rce1p [Saccharomyces cerevisiae S288c] [gi:6323930] | | PubMed | | | Data Table |  |
|
| 46 | [SID26730032] | Inactive | | | uHTS identification of small molecule inhibitors of tim23-1 yeast via a luminescent assay [AID463212, Type: screening] | TPA: Tim23p [Saccharomyces cerevisiae S288c] [gi:285814664] |  View X | Row No. | 46 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of tim23-1 yeast via a luminescent assay | | AID | 463212 | | BioAssay type | screening | | Target | TPA: Tim23p [Saccharomyces cerevisiae S288c] [gi:285814664] | | PubMed | | | Data Table |  |
|
| 47 | [SID26730032] | Inactive | | | HTS of Small Molecules that Regulate V-ATPase Proton Transport in Yeast using pHLuorin [AID504577, Type: screening] | Vma11p [Saccharomyces cerevisiae S288c] [gi:6325022] |  View X | Row No. | 47 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | HTS of Small Molecules that Regulate V-ATPase Proton Transport in Yeast using pHLuorin | | AID | 504577 | | BioAssay type | screening | | Target | Vma11p [Saccharomyces cerevisiae S288c] [gi:6325022] | | PubMed | | | Data Table |  |
|
| 48 | [SID26730032] | Inactive | | | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay [AID463190, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 48 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent assay | | AID | 463190 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
|
| 49 | [SID26730032] | Inactive | | | uHTS identification of small molecule inhibitors of tim10 yeast via a luminescent assay [AID463195, Type: screening] | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] |  View X | Row No. | 49 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | uHTS identification of small molecule inhibitors of tim10 yeast via a luminescent assay | | AID | 463195 | | BioAssay type | screening | | Target | TPA: Tim10p [Saccharomyces cerevisiae S288c] [gi:285809906] | | PubMed | | | Data Table |  |
|
| 50 | [SID26730032] | Inactive | | | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the membrane-associated serine protease Rv3671c in M.tuberculosis [AID2606, Type: screening] | membrane-associated serine protease [Mycobacterium tuberculosis H37Rv] [gi:15610807] |  View X | Row No. | 50 | | Structure |
| | Substance | | | SID | 26730032 | | CID | 2741318 | | Outcome | Inactive | | BioAssay | Fluorescence polarization-based primary biochemical high throughput screening assay to identify inhibitors of the membrane-associated serine protease Rv3671c in M.tuberculosis | | AID | 2606 | | BioAssay type | screening | | Target | membrane-associated serine protease [Mycobacterium tuberculosis H37Rv] [gi:15610807] | | PubMed | | | Data Table |  |
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